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Mutated KCNQ1 activates hereditary long QT syndromes. 1 / 1

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"The mutations of KCNQ1 have been known to cause hereditary long QT syndromes, which are characterized by the prolongation of QT intervals on the electrocardiogram; in some instances, these syndromes cause sudden cardiac death in the young through the loss of function of the potassium channel in the heart."

20056949

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Mutated KCNQ1 activates hereditary long QT syndromes. 1 / 1

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